van der Heijden Lizz, Dijkstra P D Sander, Blay Jean-Yves, Gelderblom Hans
Department of Orthopedic Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Department of Medical Oncology, Centre Leon Berard, Lyon, France.
Eur J Cancer. 2017 May;77:75-83. doi: 10.1016/j.ejca.2017.02.021. Epub 2017 Mar 30.
Giant cell tumour of bone (GCTB) is an intermediate locally aggressive primary bone tumour, occurring mostly at the meta-epiphysis of long bones. Overexpression of receptor activator of nuclear factor kappa-B ligand (RANKL) by mononuclear neoplastic stromal cells promotes recruitment of numerous reactive multinucleated osteoclast-like giant cells, causing lacunar bone resorption. Preferential treatment is curettage with local adjuvants such as phenol, alcohol or liquid nitrogen. The remaining cavity may be filled with bone graft or polymethylmethacrylate (PMMA) bone cement; benefits of the latter are a lower risk of recurrence, possibility of direct weight bearing and early radiographic detection of recurrences. Reported recurrence rates are comparable for the different local adjuvants (27-31%). Factors increasing the local recurrence risk include soft tissue extension and anatomically difficult localisations such as the sacrum. When joint salvage is impossible, en-bloc resection and endoprosthetic joint replacement may be performed. Local tumour control on the one hand and maintenance of a functional native joint and quality of life on the other hand are the main pillars of surgical treatment for this disease. Current knowledge and development in the fields of imaging, functional biology and systemic therapy are forcing us into a paradigm shift from a purely surgical approach towards a multidisciplinary approach. Systemic therapy with denosumab (RANKL inhibitor) or zoledronic acid (bisphosphonates) blocks, respectively inhibits, bone resorption by osteoclast-like giant cells. After use of zoledronic acid, stabilisation of local and metastatic disease has been reported, although the level of evidence is low. Denosumab is more extensively studied in two prospective trials, and appears effective for the optimisation of surgical treatment. Denosumab should be considered in the standard multidisciplinary treatment of advanced GCTB (e.g. cortical destruction, soft tissue extension, joint involvement or sacral localisation) to facilitate surgery at a later stage, and thereby aiming at immediate local control. Even though several questions concerning optimal treatment dose, duration and interval and drug safety remain unanswered, denosumab is among the most effective drug therapies in oncology.
骨巨细胞瘤(GCTB)是一种具有局部侵袭性的中间型原发性骨肿瘤,多发生于长骨的干骺端。单核肿瘤性基质细胞中核因子κB受体活化因子配体(RANKL)的过表达促进了大量反应性多核破骨细胞样巨细胞的募集,导致骨陷窝吸收。首选治疗方法是刮除术,并辅以苯酚、酒精或液氮等局部辅助剂。剩余的骨腔可用骨移植材料或聚甲基丙烯酸甲酯(PMMA)骨水泥填充;后者的优点是复发风险较低、可直接负重以及能在影像学上早期发现复发。不同局部辅助剂的报告复发率相当(27% - 31%)。增加局部复发风险的因素包括软组织受累以及解剖部位困难的情况,如骶骨。当无法保留关节时,可进行整块切除和人工关节置换。一方面实现局部肿瘤控制,另一方面维持天然关节功能和生活质量,是该疾病外科治疗的主要支柱。影像学、功能生物学和全身治疗领域的现有知识和进展正促使我们从单纯的手术方法向多学科方法转变。使用地诺单抗(RANKL抑制剂)或唑来膦酸(双膦酸盐)进行全身治疗分别阻断或抑制破骨细胞样巨细胞的骨吸收。使用唑来膦酸后,虽证据水平较低,但已有局部和转移性疾病得到稳定的报告。地诺单抗在两项前瞻性试验中得到了更广泛的研究,并且似乎对优化手术治疗有效。在晚期GCTB(如皮质破坏、软组织受累、关节受累或骶骨部位)的标准多学科治疗中应考虑使用地诺单抗,以便在后期便于手术,从而实现立即的局部控制。尽管关于最佳治疗剂量、持续时间、间隔和药物安全性的几个问题仍未得到解答,但地诺单抗是肿瘤学中最有效的药物治疗方法之一。